Histopathological Growth Pattern in Colorectal Liver Metastasis and The Tumor Immune Microenvironment

Cancers (Basel). 2022 Dec 28;15(1):181. doi: 10.3390/cancers15010181.

Abstract

Almost half of all patients with colorectal cancer present with or eventually develop metastasis, most frequently in the liver. Understanding the histopathological growth patterns and tumor immune microenvironment of colorectal liver metastases may help determine treatment strategies and assess prognosis. A literature search was conducted to gather information on cancer biology, histopathological growth patterns, and the tumor immune microenvironment in colorectal liver metastases, including their mechanisms and their impact on clinical outcomes. A first consensus on histopathological growth patterns emerged in 2017, identifying five growth patterns. Later studies found benefits from a two-tier system, desmoplastic and non-desmoplastic, incorporated into the updated 2022 consensus. Furthermore, the tumor immune microenvironment shows additional characteristic features with relevance to cancer biology. This includes density of T-cells (CD8+), expression of claudin-2, presence of vessel co-option versus angiogenesis, as well as several other factors. The relation between histopathological growth patterns and the tumor immune microenvironment delineates distinct subtypes of cancer biology. The distinct subtypes are found to correlate with risk of metastasis or relapse, and hence to clinical outcome and long-term survival in each patient. In order to optimize personalized and precision therapy for patients with colorectal liver metastases, further investigation into the mechanisms of cancer biology and their translational aspects to novel treatment targets is warranted.

Keywords: angiogenesis; chemotherapy; colorectal cancer; growth pattern; hepatic metastases; histopathology; immune system; invasive front; liver metastasis; pathology; recurrence; tumor microenvironment.

Publication types

  • Review

Grants and funding

Funded in part by Folke Hermansen Cancer Fund, an unrestricted intramural grant from Stavanger University Hospital, and a research grant from Helse Vest (#F-12625).